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针对研究不足的人类基因进行系统性研究欺诈的可能性:原因、后果及潜在解决方案

The Possibility of Systematic Research Fraud Targeting Under-Studied Human Genes: Causes, Consequences, and Potential Solutions.

作者信息

Byrne Jennifer A, Grima Natalie, Capes-Davis Amanda, Labbé Cyril

机构信息

Molecular Oncology Laboratory, Children's Cancer Research Unit, Kids Research, The Children's Hospital at Westmead, Westmead, NSW, Australia.

Discipline of Child and Adolescent Health, The University of Sydney and The Children's Hospital at Westmead, Westmead, NSW, Australia.

出版信息

Biomark Insights. 2019 Feb 5;14:1177271919829162. doi: 10.1177/1177271919829162. eCollection 2019.

Abstract

A major reason for biomarker failure is the selection of candidate biomarkers based on inaccurate or incorrect published results. Incorrect research results leading to the selection of unproductive biomarker candidates are largely considered to stem from unintentional research errors. The additional possibility that biomarker research may be actively misdirected by research fraud has been given comparatively little consideration. This review discusses what we believe to be a new threat to biomarker research, namely, the possible systematic production of fraudulent gene knockdown studies that target under-studied human genes. We describe how fraudulent papers may be produced in series by paper mills using what we have described as a 'theme and variations' model, which could also be considered a form of salami slicing. We describe features of these single-gene knockdown publications that may allow them to evade detection by journal editors, peer reviewers, and readers. We then propose a number of approaches to facilitate their detection, including improved awareness of the features of publications constructed in series, broader requirements to post submitted manuscripts to preprint servers, and the use of semi-automated literature screening tools. These approaches may collectively improve the detection of fraudulent studies that might otherwise impede future biomarker research.

摘要

生物标志物研究失败的一个主要原因是基于不准确或错误的已发表结果来选择候选生物标志物。导致选择无成效的生物标志物候选物的错误研究结果在很大程度上被认为源于无意的研究错误。生物标志物研究可能被研究欺诈蓄意误导的额外可能性相对而言很少受到关注。本综述讨论了我们认为对生物标志物研究的一种新威胁,即针对研究较少的人类基因可能系统性地产生欺诈性基因敲低研究。我们描述了论文工厂如何使用我们所称的“主题与变体”模型串联炮制欺诈性论文,这也可被视为一种切香肠策略。我们描述了这些单基因敲低出版物可能使其逃避期刊编辑、同行评审人员和读者检测的特征。然后我们提出了一些便于检测它们的方法,包括提高对串联构建的出版物特征的认识、将提交的稿件发布到预印本服务器的更广泛要求,以及使用半自动文献筛选工具。这些方法可能共同提高对可能阻碍未来生物标志物研究的欺诈性研究的检测。

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